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A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencing.
Behjati, Sam; Maschietto, Mariana; Williams, Richard D; Side, Lucy; Hubank, Mike; West, Rebecca; Pearson, Katie; Sebire, Neil; Tarpey, Patrick; Futreal, Andrew; Brooks, Tony; Stratton, Michael R; Anderson, John.
Afiliación
  • Behjati S; Cancer Genome Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom; Department of Paediatrics, University of Cambridge, Cambridge, United Kingdom.
  • Maschietto M; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
  • Williams RD; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
  • Side L; Departments of Clinical Genetics, Great Ormond Street Hospital, London, United Kingdom.
  • Hubank M; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
  • West R; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
  • Pearson K; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
  • Sebire N; Departments of Histopathology, Great Ormond Street Hospital, London, United Kingdom.
  • Tarpey P; Department of Paediatrics, University of Cambridge, Cambridge, United Kingdom.
  • Futreal A; Department of Paediatrics, University of Cambridge, Cambridge, United Kingdom.
  • Brooks T; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
  • Stratton MR; Cancer Genome Project, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
  • Anderson J; Unit of Molecular Haematology and Cancer Biology, UCL Institute of Child Health, London, United Kingdom.
PLoS One ; 9(5): e96531, 2014.
Article en En | MEDLINE | ID: mdl-24810334
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteína p53 Supresora de Tumor / Síndrome de Li-Fraumeni / Mutación de Línea Germinal Límite: Child, preschool / Humans / Infant / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteína p53 Supresora de Tumor / Síndrome de Li-Fraumeni / Mutación de Línea Germinal Límite: Child, preschool / Humans / Infant / Male Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido